Conference Compendium

Medical Device Validation Week 2017

This year's Medical Device Validation Week on March 28-30, 2017 in Minneapolis, MN focused on design control and process verification and validation, as pertaining to medical devices. With this compendium, you will access content tailored to hone in on medical device validation and quality challenges.

Topics Include:

  • Preparing and conducting test method validation, achieving advanced risk management strategies for design, process and product validation
  • Managing change control process enterprise-wide
  • Building a site validation master plan
  • Ensuring data security and data integrity through an effective CSV system
  • Developing and utilizing expedited SOPs

There were two tracks at the event focusing on design control, and the other on process verification and validation. With this compendium, you don't have to miss a single session and you get all the benefits of receiving the content from our stellar faculty.

Subject Matter Experts Include:

  • Roberta Goode, MSBE, CQE
    President, Goode Compliance International
  • Tim Carr
    Process Validation, Non-Product Software and Inspection Manager, Beckman-Coulter
  • Asmita Khanolkar
    Manager, Manufacturing Engineering, Cequr
  • George Omae
    Senior Engineering Manager, Medtronic
  • And many others!

This content is only available to IVT members.
Get help maintaining your knowledge . Read More!

If you are already a member and you do not have access to this article, upgrade your membership.
Need help? Read our FAQs.




Product Added Successfully

This product has been added to your account and you can access it from your dashboard. As a member, you are entitled to a total of 0 products.

Do you want access to more of our products? Upgrade your membership now!

Your Product count is over the limit

Do you want access to more of our products? Upgrade your membership now!

Product added to cart successfully.

You can continue shopping or proceed to checkout.